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268909

Sigma-Aldrich

cis-3,7-Dimethyl-2,6-octadien-1-ol

97%

Synonym(e):

Nerol, cis-3,7-Dimethyl-2,6-octadien-1-ol

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About This Item

Lineare Formel:
(CH3)2C=CHCH2CH2C(CH3)=CHCH2OH
CAS-Nummer:
106-25-2
Molekulargewicht:
154.25
Beilstein:
1722455
EG-Nummer:
203-378-7
MDL-Nummer:
MFCD00063204
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24856300
NACRES:
NA.22

Qualitätsniveau

100

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.474 (lit.)

bp

103-105 °C/9 mmHg (lit.)

Löslichkeit

absolute ethanol: soluble(lit.)

Dichte

0.876 g/mL at 25 °C (lit.)

Funktionelle Gruppe

hydroxyl

SMILES String

C\C(C)=C\CC\C(C)=C/CO

InChI

1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7-

InChIKey

GLZPCOQZEFWAFX-YFHOEESVSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

The antifungal efficacy of nerol (cis-3,7-Dimethyl-2,6-octadien-1-ol), against Aspergillus flavus, was studied.

Anwendung

cis-3,7-Dimethyl-2,6-octadien-1-ol was used in the highly convergent and stereocontrolled synthesis of epothilone D.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1B

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

226.0 °F - closed cup

Flammpunkt (°C)

107.78 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
SHBQ1123
SHBN0144
SHBM9268
SHBM8860
SHBL5868

Die passende Version wird nicht angezeigt?

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Malathion European Pharmacopoeia (EP) Reference Standard

M0120000

Malathion

(±)-Citronellal ≥95.0% (GC)

Sigma-Aldrich

27470

(±)-Citronellal

Geranylbromid 95%

Sigma-Aldrich

329118

Geranylbromid

Citral natural, ≥96%, FCC, FG

Sigma-Aldrich

W230316

Citral

D-Carvon ≥96%, FG

Sigma-Aldrich

W224928

D-Carvon

Jun Tian et al.
TheScientificWorldJournal, 2013, 230795-230795 (2014-01-24)
The antifungal efficacy of nerol (NEL) has been proved against Aspergillus flavus by using in vitro and in vivo tests. The mycelial growth of A. flavus was completely inhibited at concentrations of 0.8 μ L/mL and 0.1 μ L/mL NEL
Ludger A Wessjohann et al.
The Journal of organic chemistry, 78(21), 10588-10595 (2013-10-02)
A highly convergent and stereocontrolled synthesis of epothilone D (4) is reported. Key features are a cheap and Z-selective synthesis of the northern half based on nerol and acetoacetate and chromium(II)-mediated Reformatsky reactions as a powerful tool for chemoselective asymmetric
Bertrand Fouks et al.
The Journal of experimental biology, 216(Pt 2), 285-291 (2012-10-06)
Foraging is a result of innate and acquired mechanisms, and is optimized in order to increase fitness. During foraging, an animal faces many threats, such as predation and infection. The uptake of parasites and diseases while foraging is common and
Yukihiro Yamamoto et al.
Bioorganic & medicinal chemistry letters, 18(14), 4044-4046 (2008-06-17)
In order to prepare functional phospholipids in the medical and pharmaceutical fields, perillyl alcohol, myrtenol, and nerol were transphosphatidylated via phospholipase D in an aqueous system. The yields of phosphatidyl-perillyl alcohol, -myrtenol, and -nerol were 79 mol %, 87 mol
Pankaj K Sharma et al.
Plant science : an international journal of experimental plant biology, 203-204, 63-73 (2013-02-19)
Plants synthesize volatile alcohol esters on environmental insult or as metabolic induction during flower/fruit development. However, essential oil plants constitutively produce them as the oil constituents. Their synthesis is catalyzed by BAHD family enzymes called alcohol acyltransferases (AATs). However, no
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